Glucagon-like peptide-1 agonists combined with sodium-glucose cotransporter-2 inhibitors reduce weight in type 1 diabetes.


Journal

Obesity (Silver Spring, Md.)
ISSN: 1930-739X
Titre abrégé: Obesity (Silver Spring)
Pays: United States
ID NLM: 101264860

Informations de publication

Date de publication:
03 2023
Historique:
revised: 02 11 2022
received: 12 09 2022
accepted: 22 11 2022
entrez: 22 2 2023
pubmed: 23 2 2023
medline: 25 2 2023
Statut: ppublish

Résumé

This study evaluated whether adding sodium-glucose cotransporter-2 inhibitors (SGLT2i) and/or glucagon-like peptide-1 receptor agonists (GLP1-RA) to insulin reduced weight and glycemia in people with type 1 diabetes. This retrospective analysis of electronic health records evaluated 296 people with type 1 diabetes over 12 months after medications were first prescribed. Four groups were defined: control n = 80, SGLT2i n = 94, GLP1-RA n = 82, and combination of drugs (Combo) n = 40. We measured changes at 1 year in weight and glycated hemoglobin (HbA1c). The control group did not have changes in weight or glycemic control. The mean (SD) percentage weight loss after 12 months was 4.4% (6.0%), 8.2%  (8.5%), and 9.0% (8.4%) in the SGLT2i, GLP1-RA, and Combo groups, respectively (p < 0.001). The Combo group lost the most weight (p < 0.001). The HbA1c reduction was 0.4%  (0.7%), 0.3% (0.7%), and 0.6% (0.8%) in the SGLT2i, GLP1-RA, and Combo groups, respectively (p < 0.001). The Combo group had the biggest improvements in glycemic control and total and low-density lipoprotein cholesterol compared with baseline (all p < 0.01). Severe adverse events were similar between all the groups, with no increased risk of diabetic ketoacidosis. The SGLT2i and GLP1-RA agents on their own improved body weight and glycemia, but combining the medications resulted in more weight loss. Treatment intensification appears to result in benefits with no difference in severe adverse events.

Identifiants

pubmed: 36811241
doi: 10.1002/oby.23677
doi:

Substances chimiques

Hypoglycemic Agents 0
Sodium-Glucose Transporter 2 Inhibitors 0
Glycated Hemoglobin 0
Glucagon-Like Peptide-1 Receptor 0
Glucagon-Like Peptide 1 89750-14-1
Glucose IY9XDZ35W2
Sodium 9NEZ333N27

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

716-723

Informations de copyright

© 2023 The Authors. Obesity published by Wiley Periodicals LLC on behalf of The Obesity Society.

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Auteurs

Ebaa Al-Ozairi (E)

Dasman Diabetes Institute, Kuwait City, Kuwait.
Department of Medicine, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.

Mohammad Irshad (M)

Dasman Diabetes Institute, Kuwait City, Kuwait.

Etab Taghadom (E)

Dasman Diabetes Institute, Kuwait City, Kuwait.

Litty Sojan (L)

Dasman Diabetes Institute, Kuwait City, Kuwait.

Jumana Al Kandari (J)

Dasman Diabetes Institute, Kuwait City, Kuwait.

Dherar Alroudhan (D)

Dasman Diabetes Institute, Kuwait City, Kuwait.

Carel W le Roux (CW)

Diabetes Complications Research Center, UCD Conway Institute, University College Dublin School of Medicine, Dublin, Ireland.
Diabetes Research Centre, Ulster University, Coleraine, UK.

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